dc.contributor.author | Beloqui Elizazu, Ana | |
dc.contributor.author | Mane, Shivshankar R. | |
dc.contributor.author | Langer, Marcel | |
dc.contributor.author | Glassner, Mathias | |
dc.contributor.author | Bauer, Dennis M. | |
dc.contributor.author | Fruk, Ljiljana | |
dc.contributor.author | Barner-Kowollik, Christopher | |
dc.contributor.author | Delaittre, Guillaume | |
dc.date.accessioned | 2021-03-04T09:28:45Z | |
dc.date.available | 2021-03-04T09:28:45Z | |
dc.date.issued | 2020-11-02 | |
dc.identifier.citation | Angewandte Chemie International Edition 59(45) : 19951-19955 (2020) | es_ES |
dc.identifier.issn | 1433-7851 | |
dc.identifier.issn | 1521-3773 | |
dc.identifier.uri | http://hdl.handle.net/10810/50462 | |
dc.description.abstract | We introduce the bioconjugation of polymers synthesized by RAFT polymerization, bearing no specific functional end group, by means of hetero-Diels-Alder cycloaddition through their inherent terminal thiocarbonylthio moiety with a diene-modified model protein. Quantitative conjugation occurs over the course of a few hours, at ambient temperature and neutral pH, and in the absence of any catalyst. Our technology platform affords thermoresponsive bioconjugates, whose aggregation is solely controlled by the polymer chains. | es_ES |
dc.description.sponsorship | A.B. thanks the Spanish Research Agency (AEI) for funds within the RamonyCajal program (RYC2018-025923-I) and Retos call (PID2019-110239RB-I00). C.B.-K. acknowledges funding by the Australian Research Council (ARC) in the context of a Laureate Fellowship and continued key support from the Queensland University of Technology (QUT) via its Centre for Materials Science. G.D. thanks the German Federal Ministry of Education and Research (BMBF, Grant No. 031A095C) for funding (Molecular Interaction Engineering program, Biotechnologie 2020+). The Levkin lab (IBCS, KIT) is thanked for access to DLS. Frank Kirschhofer, Boris Kuhl, and Dr Gerald Brenner-Weiss (IFG, KIT) are acknowledged for providing access to and support on MALDI-ToF spectrometry. Open access funding enabled and organized by Projekt DEAL. | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Wiley | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/RYC2018-025923-I | es_ES |
dc.relation | info:eu-repo/grantAgreement/MICINN/PID2019-110239RB-I00 | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | * |
dc.subject | bioconjugation | es_ES |
dc.subject | Diels-Alder cycloaddition | es_ES |
dc.subject | end group | es_ES |
dc.subject | polymer | es_ES |
dc.subject | protein | es_ES |
dc.subject | conjugation | es_ES |
dc.subject | stability | es_ES |
dc.subject | glycol | es_ES |
dc.subject | well | es_ES |
dc.subject | polymerization | es_ES |
dc.subject | copolymers | es_ES |
dc.subject | chemistry | es_ES |
dc.subject | behavior | es_ES |
dc.subject | design | es_ES |
dc.subject | drug | es_ES |
dc.title | Hetero-Diels-Alder Cycloaddition with RAFT Polymers as Bioconjugation Platform | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.rights.holder | This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0) | es_ES |
dc.rights.holder | Atribución 3.0 España | * |
dc.relation.publisherversion | https://onlinelibrary.wiley.com/doi/10.1002/anie.202005747 | es_ES |
dc.identifier.doi | 10.1002/anie.202005747 | |
dc.departamentoes | Química aplicada | es_ES |
dc.departamentoeu | Kimika aplikatua | es_ES |